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The aryl hydrocarbon receptor regulates nucleolar activity and protein synthesis in MYC-expressing cells

MYC enhances protein synthesis by regulating genes involved in ribosome biogenesis and protein translation. Here, we show that MYC-induced protein translation is mediated by the transcription factor aryl hydrocarbon receptor (AHR), which is induced by MYC in colonic cells. AHR promotes protein synth...

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Detalles Bibliográficos
Autores principales: Lafita-Navarro, M. Carmen, Kim, Min, Borenstein-Auerbach, Nofit, Venkateswaran, Niranjan, Hao, Yi-Heng, Ray, Roshni, Brabletz, Thomas, Scaglioni, Pier Paolo, Shay, Jerry W., Conacci-Sorrell, Maralice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6169836/
https://www.ncbi.nlm.nih.gov/pubmed/30254109
http://dx.doi.org/10.1101/gad.313007.118
Descripción
Sumario:MYC enhances protein synthesis by regulating genes involved in ribosome biogenesis and protein translation. Here, we show that MYC-induced protein translation is mediated by the transcription factor aryl hydrocarbon receptor (AHR), which is induced by MYC in colonic cells. AHR promotes protein synthesis by activating the transcription of genes required for ribosome biogenesis and protein translation, including OGFOD1 and NOLC1. Using surface sensing of translation (SUnSET) to measure global protein translation, we found that silencing AHR or its targets diminishes protein synthesis. Therefore, targeting AHR or its downstream pathways could provide a novel approach to limit biomass production in MYC-driven tumors.